BLM Products U. Vertriebsges Recall: BLM Prod.-und Vertriebsges.mbH & Co. KG has initiated a voluntary recall of Priano Rosso Pesto Sauce, 6.7 oz. packaged in glass jars due to undeclared allergens egg and milk. - F-1548-2018

🇺🇸 United States

1. May 15, 2018 - Recall initiated
2. June 13, 2018 - Reported by source
3. October 11, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1548-2018

Event ID

80117

Status

Terminated

Classification

Class I

Company

BLM Products U. Vertriebsges

Product description

Priano Rosso Pesto Sauce, 6.7oz glass jar

Quantity

174636 jars

Reason

BLM Prod.-und Vertriebsges.mbH & Co. KG has initiated a voluntary recall of Priano Rosso Pesto Sauce, 6.7 oz. packaged in glass jars due to undeclared allergens egg and milk.

Recall initiation date

May 15, 2018

Report date

June 13, 2018

Classification date

Not published in this source record

Termination date

October 11, 2018

Distribution pattern

Domestic only: Arkansas, California, Connecticut, District of Columbia, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Maryland, Massachusetts, Michigan, Missouri, North Carolina, Nebraska, New Hampshire, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Virginia, Vermont, and West Virginia

UPC, lot, and code information

Lot Code Best-Buy Date LA 016 07-16-2019, 07-01-2019 LA 017 07-17-2019, 07-01-2019, 09-17-2019 LA 052 08-21-2019 LA 053 08-22-2019 LA 085 09-26-2019 LAB 312 05-08-2019 LAB 324 05-20-2019 LAB 325 05-21-2019

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: BLM Products U. Vertriebsges

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of October 11, 2018.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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